WO2017223030A1 - Composition lubrifiante - Google Patents

Composition lubrifiante Download PDF

Info

Publication number
WO2017223030A1
WO2017223030A1 PCT/US2017/038240 US2017038240W WO2017223030A1 WO 2017223030 A1 WO2017223030 A1 WO 2017223030A1 US 2017038240 W US2017038240 W US 2017038240W WO 2017223030 A1 WO2017223030 A1 WO 2017223030A1
Authority
WO
WIPO (PCT)
Prior art keywords
composition
antioxidant
lubricant composition
hindered phenolic
sulphide
Prior art date
Application number
PCT/US2017/038240
Other languages
English (en)
Inventor
Martin R. Greaves
Evelyn A. ZAUGG-HOOZEMANS
Original Assignee
Dow Global Technologies Llc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Dow Global Technologies Llc filed Critical Dow Global Technologies Llc
Priority to US16/310,310 priority Critical patent/US10844312B2/en
Priority to EP17733720.1A priority patent/EP3475400B1/fr
Priority to CN201780039000.4A priority patent/CN109415650B/zh
Priority to JP2018566592A priority patent/JP2019522706A/ja
Priority to BR112018076938A priority patent/BR112018076938A2/pt
Publication of WO2017223030A1 publication Critical patent/WO2017223030A1/fr

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M169/00—Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
    • C10M169/04—Mixtures of base-materials and additives
    • C10M169/044—Mixtures of base-materials and additives the additives being a mixture of non-macromolecular and macromolecular compounds
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M141/00—Lubricating compositions characterised by the additive being a mixture of two or more compounds covered by more than one of the main groups C10M125/00 - C10M139/00, each of these compounds being essential
    • C10M141/08—Lubricating compositions characterised by the additive being a mixture of two or more compounds covered by more than one of the main groups C10M125/00 - C10M139/00, each of these compounds being essential at least one of them being an organic sulfur-, selenium- or tellurium-containing compound
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M161/00—Lubricating compositions characterised by the additive being a mixture of a macromolecular compound and a non-macromolecular compound, each of these compounds being essential
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M169/00—Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
    • C10M169/04—Mixtures of base-materials and additives
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M169/00—Lubricating compositions characterised by containing as components a mixture of at least two types of ingredient selected from base-materials, thickeners or additives, covered by the preceding groups, each of these compounds being essential
    • C10M169/04—Mixtures of base-materials and additives
    • C10M169/041—Mixtures of base-materials and additives the additives being macromolecular compounds only
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2203/00—Organic non-macromolecular hydrocarbon compounds and hydrocarbon fractions as ingredients in lubricant compositions
    • C10M2203/10—Petroleum or coal fractions, e.g. tars, solvents, bitumen
    • C10M2203/1006—Petroleum or coal fractions, e.g. tars, solvents, bitumen used as base material
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2205/00—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions
    • C10M2205/02—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers
    • C10M2205/028—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers containing aliphatic monomers having more than four carbon atoms
    • C10M2205/0285—Organic macromolecular hydrocarbon compounds or fractions, whether or not modified by oxidation as ingredients in lubricant compositions containing acyclic monomers containing aliphatic monomers having more than four carbon atoms used as base material
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/02—Hydroxy compounds
    • C10M2207/023—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings
    • C10M2207/026—Hydroxy compounds having hydroxy groups bound to carbon atoms of six-membered aromatic rings with tertiary alkyl groups
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2207/00—Organic non-macromolecular hydrocarbon compounds containing hydrogen, carbon and oxygen as ingredients in lubricant compositions
    • C10M2207/28—Esters
    • C10M2207/287—Partial esters
    • C10M2207/289—Partial esters containing free hydroxy groups
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
    • C10M2209/105—Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing three carbon atoms only
    • C10M2209/1055—Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing three carbon atoms only used as base material
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2209/00—Organic macromolecular compounds containing oxygen as ingredients in lubricant compositions
    • C10M2209/10—Macromolecular compoundss obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2209/103—Polyethers, i.e. containing di- or higher polyoxyalkylene groups
    • C10M2209/106—Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing four carbon atoms only
    • C10M2209/1065—Polyethers, i.e. containing di- or higher polyoxyalkylene groups of alkylene oxides containing four carbon atoms only used as base material
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2219/00—Organic non-macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2219/08—Thiols; Sulfides; Polysulfides; Mercaptals
    • C10M2219/082—Thiols; Sulfides; Polysulfides; Mercaptals containing sulfur atoms bound to acyclic or cycloaliphatic carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10M—LUBRICATING COMPOSITIONS; USE OF CHEMICAL SUBSTANCES EITHER ALONE OR AS LUBRICATING INGREDIENTS IN A LUBRICATING COMPOSITION
    • C10M2221/00—Organic macromolecular compounds containing sulfur, selenium or tellurium as ingredients in lubricant compositions
    • C10M2221/04—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • C10M2221/043—Polyoxyalkylene ethers with a thioether group
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2030/00—Specified physical or chemical properties which is improved by the additive characterising the lubricating composition, e.g. multifunctional additives
    • C10N2030/10—Inhibition of oxidation, e.g. anti-oxidants
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00—Specified use or application for which the lubricating composition is intended
    • C10N2040/04—Oil-bath; Gear-boxes; Automatic transmissions; Traction drives
    • C10N2040/042—Oil-bath; Gear-boxes; Automatic transmissions; Traction drives for automatic transmissions
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00—Specified use or application for which the lubricating composition is intended
    • C10N2040/08—Hydraulic fluids, e.g. brake-fluids
    • C—CHEMISTRY; METALLURGY
    • C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
    • C10N—INDEXING SCHEME ASSOCIATED WITH SUBCLASS C10M RELATING TO LUBRICATING COMPOSITIONS
    • C10N2040/00—Specified use or application for which the lubricating composition is intended
    • C10N2040/25—Internal-combustion engines

Definitions

  • the present invention is related to a lubricant composition including a base oil which contains a hindered phenolic anti-oxidant and a poly ether sulphide. More specifically, the present invention relates to a lubricant composition that includes a poly ether sulphide (S-PAG) which can boost the anti-oxidant performance of the hindered phenolic anti-oxidant present in the lubricant composition.
  • S-PAG poly ether sulphide
  • lubricants Most industrial and automotive lubricants contain an anti-oxidant or a combination of anti-oxidants to extend the lubricants' useful operating life. In some applications, such as automotive engine oils, there is a need for lubricants to perform under high thermal stresses where the lubricant can experience temperatures of for example 250 degrees Celsius (°C) or higher. In addition, lubricants having longer drain intervals are desired. Currently for example, oil drain intervals for passenger cars using current motor oils require a drain interval every 3 to 6 months over the life time of the automobile.
  • One potential technical solution to extending the life or oil drain intervals of a lubricant is to develop new anti-oxidants useful in lubricants or to develop combination of current commercial anti-oxidants with other materials that provide a synergistic performance in extending oil drain intervals.
  • anti-oxidants used in lubricants are alkylated diphenylamines (ADPA).
  • ADPA alkylated diphenylamines
  • Another type of anti-oxidants used in lubricants is hindered phenolic anti-oxidants. Both of these types of anti-oxidants are often described as “free radical scavengers”. Combinations of free radical scavengers (such as an aminic and a phenolic) are known.
  • Another class of anti-oxidants are "peroxide decomposers”. The peroxide decomposer class of anti-oxidants' mode of action is very different to the mode of action of free radical scavengers. The action of the peroxide decomposers is to reduce the alkyl hydroperoxides to alcohols. These hydroperoxides form from the radical
  • peroxide decomposers are consumed in a sacrificial manner.
  • Conventional peroxide decomposers include sulphur-containing organometallic materials such as molybdenum dialkyldithiocarbamates (MoDTC) and zinc dialkyldithiophosphates (ZDDP).
  • MoDTC molybdenum dialkyldithiocarbamates
  • ZDDP zinc dialkyldithiophosphates
  • Combinations of a free radical scavenger with a peroxide decomposer are also known such as combinations of ADPA and MoDTC.
  • the primary use of organometallic-based peroxide decomposers is as surface active materials and not as anti-oxidants.
  • MoDTC is used primarily as a friction modifier.
  • ZDDPs are used primarily as anti-wear additives. Because MoDTCs and ZDDPs are surface active and chemically react with surfaces to form films, these compounds are consumed over time. The effectiveness of per
  • dialkyldithiocarbamates have been researched as an altemative to MoDTC but such dialkyldithiocarbamates, when used in hydrocarbon oils, are much less effective than MoDTC and can leave deposits on surfaces of lubrication equipment which, in turn, can impact wear of the lubrication equipment.
  • a lubricant composition that includes an antioxidant package containing an anti-oxidant booster that enhances the anti-oxidant performance of the anti-oxidants and extends the life of the lubricant.
  • the present invention is directed to an antioxidant package, which comprises a combination of a poly ether sulphide compound and a hindered phenolic anti-oxidant compound.
  • the antioxidant package of the present invention includes a combination of (i) at least one hindered phenolic antioxidant such as benzene propanoic acid, 3,5-bis(l ,l -dimethylethyl)-4-hydroxy-,C7-9- branched alkyl ester, and (ii) at least one poly ether sulphide such as an alkoxylate of bis(2- hydroxyethyl) sulphide.
  • the antioxidant package can be used in a lubricant composition such that the antioxidant package provides a remarkable synergistic performance or effect in extending the life of the lubricant composition.
  • the present invention is directed to a lubricant composition containing the above antioxidant package.
  • the lubricant composition of the present invention includes: (a) a base oil, (b) at least one hindered phenolic, and (c) at least one polyether sulphide.
  • the polyether sulphide compound (herein "S-PAG”) useful in the lubricant of the present invention provides a boost to the anti-oxidant performance of the hindered phenolic present in the lubricant of the present invention.
  • Other embodiments of the present invention include a process for preparing the antioxidant package; a process for preparing the lubricant composition containing the antioxidant package; and a process for using the lubricant composition or formulation as an automotive engine oil.
  • Base oils herein means oils that include both natural oils and synthetic oils. Natural and synthetic oils can be used in the present invention unrefined, refined, or re- refined.
  • the American Petroleum Institute (API) has defined/classified base oils into several categories (“Groups”) such as Groups I, II, III, IV and V to create guidelines for lubricant base oils.
  • Group I base stocks generally have a viscosity index of greater than or equal to (>) 80 to less than ( ⁇ ) 120 and contain greater than (>) 0.03 percent (%) sulfur and
  • Group II base stocks generally have a viscosity index of > 80 to less than
  • Group 111 base oils generally have a viscosity index > 120 and contain ⁇ 0.03 % sulfur and > 90 % saturates. ASTM D2270 is used to calculate viscosity index.
  • Group IV base oils include polvalphaolefins (PAO).
  • Group V base stocks include base stocks not included in Groups I- IV. For example, Group V base oils may include polyalkylene glycols, synthetic esters, polyisobutylenes, phosphate esters, and the like. The following table summarizes properties of each of the aforementioned five Groups of base oils.
  • an “antioxidant” herein means a component that assists in reducing the rate of oxidation of a base oil or a lubricant composition.
  • a “useful operating life”, with reference to a lubricant, herein means a lubricant having the desired functionality to be successfully used in equipment for a desired period of time.
  • antioxidant package herein means a mixture of two or more components of which at least one component is an anti-oxidant.
  • Other components useful in the antioxidant package may include, for example, one or more of the following compounds or additives:
  • the antioxidant package of the present invention includes an antioxidant component that can boost the anti-oxidant performance of antioxidants when combined with such antioxidants such as alkylated diphenyl amines (ADPA) or hindered phenolics; and that can resist being consumed as surface active materials.
  • the antioxidant package of the present invention offers a better cleanliness benefit than metal free dialkyldithiocarbamates. It is known that as lubricants age, the lubricants can form deposits which impact wear in lubrication equipment; and thus, lubricants with better cleanliness are desired.
  • poly ether backbones in some additives can provide a high level of cleanliness.
  • Functionalized polyethers (such as S-PAGs) can provide both enhanced cleanliness and the ability to boost the performance of antioxidants.
  • One broad embodiment of the present invention includes an antioxidant package useful as an antioxidant agent for a lubricating oil.
  • the antioxidant package includes a combination of: (i) at least one hindered phenolic antioxidant, and (ii) at least one poly ether sulphide.
  • a first required component (i) includes at least one hindered phenolic antioxidant compound.
  • a broad class of hindered phenolic antioxidant compounds is shown in the formula of Structure (I) as follows:
  • Ri and R 2 independently, may each be an alkyl radical having from C3 to C9 carbons; and Ry can be an alkyl radical having from C I to C30 carbons, an alkyl radical containing a carboxy group (COO) or an alkyl radical containing a thio group(-S-).
  • Structure (I) is shown in the following Structures (II) and (III), wherein n and m are each integers from 1 to 4; and R3 is an alkyl group having from 1 to 30 carbons.
  • Higher molecular weight hindered phenolic compounds represented by Structures (IV) and (V) can also be used such as those shown in Structures (IV) and (V) where Ri and R 2 can be alkyl radicals from 3 to 9 carbons; and n and m are each, individually and separately, integers from 1 to 4. These higher molecular weight hindered phenolic compounds are advantageously useful in applications where the lubricant experiences high temperatures. Higher molecular weight phenolics are typically less volatile. Examples of Rj and R 2 are when Rj and R 2 are tertiary butyl radicals.
  • the at least one hindered phenolic antioxidant compound, component (i), of the present invention can include any hindered phenolic antioxidant compound within the scope of Structure (I) above.
  • the hindered phenolic antioxidant compound of Structure (I) may include those compounds in which each Rj and R 2 , individually and separately, are C3 to C9.
  • Commercially available products which are included in Structure (I) and which are useful in the present invention may include for example, commercial products sold under the trade name IRGANOXTM which are available from BASF.
  • the hindered phenolic antioxidant can be IRGANOX LI 35 a compound commercially available from BASF.
  • IRGANOX LI 35 is an anti-oxidant and can be defined as benzene propanoic acid, 3,5-bis(l,l-dimethylethyl)-4-hydroxy-,C7-9-branched alkyl ester (CAS No. 125643-61-0).
  • IRGANOX 1076 IRGANOX 1010
  • BHT butylated hydroxy toluene
  • IRGANOX 1076 is octadecyl-3-(3,5-di-tert.butyl-4-hydroxyphenyl)- propionate (CAS No. 6683-19-8).
  • the chemical structure of IRGANOX 1076 is shown in the formula of Structure (VII) as follows:
  • IRGANOX 1010 is pentaerythritol tetrakis(3-(3,5-di-tert-butyl-4- hydroxyphenyl)propionate) and CAS No. is 6683-19-8.
  • IRGANOX 1010 is 531 g/mol.
  • the chemical structure of IRGANOX 1010 is shown i formula of Structure (VIII) as follows:
  • BHT butylated hydroxy toluene
  • the concentration of the hindered phenolic antioxidant, component (i), present in the antioxidant package of the present invention may range generally from about 1 weight percent (wt %) to about 99 wt % in one embodiment, from about 5 wt % to about 80 wt % in another embodiment, from about 5 wt % to about 50 wt % in another embodiment, from about 50 wt % to about 80 wt % in another embodiment, and from about 10 wt % to about 20 wt % in still another embodiment based on the total weight of the components in the antioxidant package.
  • the hindered phenolic antioxidant, component (i) provides the antioxidant package of the present invention with several benefit(s) including, for example, the functionality of the hindered phenolic to act as an anti-oxidant, to improve the thermo- oxi dative stability of the base oil, and to extend the base oil's useful operating life by extending oil drain intervals.
  • a second required component (ii) includes at least one polyether sulphide compound (e.g., S-PAG).
  • the at least one polyether sulphide compound, component (ii), of the present invention can be any conventional polyether sulphide compound.
  • general examples of component (ii) may include one or more of poly ethers containing a sulphur group;
  • the sulphur compound is a compound having a sulphur group in oxidation state II.
  • the polymers are known as polyether sulphoxides and the sulphur is bonded to an oxygen atom and two carbons atoms from the polyether fragments.
  • polymers have sulphur in oxidation state VI, the polymers are known as polyether sulphones and the sulphur is bonded to two oxygen atoms and two carbon atoms from the polyether fragments.
  • Polyether sulphoxides and polyether sulphones can function as anti-oxidant boosters for the hindered phenolic antioxidant.
  • polyether sulphide compound, component (ii) can be for example one or more S-PAGs which are a broad class of polyethers containing sulphur.
  • the S-PAGs useful as component (ii) are alkoxylates of thiodiglycol also known as bis(2 -hydroxy ethyl) sulphide, and 2,2'-thiodiethanol, and mixtures thereof.
  • Other bis(2-hydroxyalkyl) sulphides useful in the present invention may include for example bis(2-hydroxypropyl) sulphide, bis(2- hydroxybutyl) sulphide, bis(2-hydroxypentyl) sulphide, and mixtures thereof.
  • the polyether sulphide compound may also include disulphides such as for example alkoxylates of dithiodiglycol and mixtures of disulphides.
  • the concentration of the polyether sulphide compound, component (ii), present in the antioxidant package of the present invention may range generally from about 1 wt % to about 99 wt % in one embodiment, and from about 5 wt % to about 95 wt % in another embodiment, from about 10 wt % to about 90 wt % in yet another embodiment and from about 50 wt % to about 90 wt % in still another embodiment, based on the total weight of the components in the antioxidant package.
  • the antioxidant composition of the present invention includes a weight ratio of the hindered phenolic to the poly ether sulphide of from about 10: 1 to about 1 : 10.
  • the antioxidant composition of the present invention includes a weight ratio of the hindered phenolic to the poly ether sulphide of from about 5: 1 to about 1 : 1.
  • the poly ether sulphide compound, component (ii) provides the antioxidant package of the present invention with several benefit(s) including, for example, the functionality of the poly ether sulphide to act as an anti-oxidant booster to the hindered phenolic antioxidant.
  • the polyether sulphide compound can also improve the detergency properties of the lubricant.
  • the polyether sulphide is a low-viscosity oil and can also improve handling of the antioxidant package.
  • the viscosity of the polyether sulphide can be from about 30 centistokes (cSt) to about 150 cSt when measured using the procedure described in ASTM D445 (2015) at 40 °C.
  • the antioxidant package of the present invention may also include various other components, adjuvants, or additives including for example one or more of corrosion inhibitors, viscosity modifiers, emulsifiers, demulsifiers, dispersants, detergents, anti-wear additives, lubricity additives and extreme pressure additives, and mixtures thereof.
  • the anti-oxidant package may also contain a solvent such as a mineral oil, glycol ether, ester, polyalkylene glycol, and mixtures thereof to improve ease of handling the anti-oxidant package.
  • the concentration of the optional additives added to the antioxidant package of the present invention may range generally from 0 wt % to about 95 wt % in one embodiment, from about 0.01 wt % to about 50 wt % in another embodiment, and from about 0.1 wt % to about 20 wt % in still another embodiment, based on the total weight of the components in the antioxidant package.
  • the optional additives, component (iii), may be added to the antioxidant package to provide the antioxidant package with the function of said additives and several benefit(s).
  • corrosion inhibitors will provide ferrous and non-ferrous corrosion inhibition functionality of the final lubricant composition to which the additive package is added.
  • Viscosity modifiers can improve the viscosity index of the final lubricant composition to which the additive package is added.
  • Solvents can improve low temperature properties of the anti-package and the final lubricant composition to which the additive package is added.
  • Demulsifiers can improve the demulsification of the final lubricant composition to which the additive package is added.
  • Antiwear and extreme pressure additives can improve the antiwear and extreme pressure properties of the final lubricant composition to which the additive package is added.
  • Lubricity additives can improve the friction control properties of the final lubricant composition to which the additive package is added.
  • the process of preparing the antioxidant package of the present invention includes blending or mixing the above components (i) and (ii) together and optionally component (iii), to form the antioxidant package.
  • the process and type of equipment used to prepare the antioxidant package of the present invention includes blending or mixing of the above components in conventional mixing equipment or vessels known in the art.
  • the preparation of the antioxidant package of the present invention is achieved by blending, in known mixing equipment, components (i) and (ii) and optionally (iii) any other desirable additives.
  • the preparation of the antioxidant package of the present invention, and/or any of the steps thereof, may be a batch or a continuous process.
  • All the above compounds of the antioxidant package are typically mixed and dispersed in a vessel at a temperature enabling the preparation of an effective antioxidant package.
  • the temperature during the mixing of the above components may be generally from about 20 °C to about 80 °C in one embodiment and from about 25 °C to about 50 °C in another embodiment.
  • the process of preparing an antioxidant package of the present invention includes, for example, the steps of: (a) loading a vessel with the poly ether sulphide; (b) adding the hindered phenolic to the vessel to form a mixture in the vessel; (c) stirring the mixture at from about 25 °C to about 50 °C for about 15 minutes (min) until the mixture in the vessel is homogeneous; and (d) allowing the resulting homogeneous mixture to cool to room temperature (about 23-25 °C).
  • step (c) above one or more of the optional additives described above may be added to the mixture in the vessel.
  • the mixture is then stirred further for about 30 min at from about 25 °C to about 80 °C until the mixture in the vessel is clear and homogeneous to the visual eye.
  • the antioxidant package of the present invention prepared by the above process exhibits several unexpected and unique properties; and imparts several
  • One of the main important properties of the antioxidant package is to provide anti-oxidancy to the lubricant composition.
  • Other properties exhibited by the antioxidant package can include for example lubricity, solvency, detergency, demulsification, emulsification, antiwear, and extreme pressure performance properties.
  • the antioxidant capability property of the antioxidant package can be measured and compared to a control sample that contains the same treat level of the hindered phenolic but does not contain a poly ether sulphide; or the same level of the polyether sulphide but does not contain the hindered phenolic.
  • the method used to measure anti-oxidant performance in a modified ASTM D2893 (Method B). In this test the modifications are such that the time of the test is extended and samples of the fluid are taken after 3, 7, 14, 20, 27, 34, 41, 48, 55, 62 and 69 days and optionally every 7 days thereafter up to about 153 days and their total acid numbers (TAN) are measured using ASTM D664- 11. When the TAN value has risen by 2.0 mgKOH/g above its initial value the fluid has reached its end point and the time recorded.
  • Another beneficial property of the antioxidant package of the present invention is its capability of providing the lubricant composition with an extended operating life.
  • the life of the lubricant can be extended by the antioxidant package.
  • the extended life of the lubricant composition can be correlated to the increase (as a percentage) of the thermo-oxidative stability property of the lubricant composition containing at least one polyether sulphide compared to a lubricant composition without containing the at least one polyether sulphide.
  • the percent increase of the thermo-oxidative stability property of a lubricant composition of the present invention can be about 100 % or greater in one embodiment, about 200 % or greater in another embodiment, and about 300 % or greater in yet another embodiment.
  • the percent increase of the thermo-oxidative stability property of the lubricant composition of the present invention can be in the range of from about 100 % to about 400 % in one embodiment and from about 100 % to about 200 % in another embodiment.
  • the life of the lubricant provided by the antioxidant package can be determined using the procedure as described in a modified version of ASTM
  • One broad embodiment of the present invention includes a lubricant composition useful as a lubricating oil for applications such as automobile oils.
  • the lubricant composition includes in combination: (a) the antioxidant package of the present invention described above which comprises (i) at least one hindered phenolic antioxidant, and (ii) at least one poly ether sulphide; and (b) at least one base oil.
  • a first required component (a) includes the antioxidant package of the present invention described above which comprises (i) at least one hindered phenolic antioxidant, and (ii) at least one poly ether sulphide.
  • the concentration of the antioxidant package, component (a), in the lubricant composition of the present invention may range generally from about 0.05 wt % to about 50 wt % in one embodiment, and from about 0.5 wt % to about 25 wt % in another
  • the hindered phenolic antioxidant can be present in the lubricant composition at a concentration of from about 0.01 wt % to about 10 wt % in one embodiment and from about 0.5 wt % to about 5 wt % in another embodiment.
  • the S-PAG can be present in the lubricant composition at a concentration of from about 0.05 wt % to about 25% in one embodiment and from about 1 wt % to about 5 wt %.
  • antioxidant, component (a) provides to the lubricant composition of the present invention the following benefit(s), for example, long life and detergency.
  • a second required component (b) includes at least one base oil.
  • the base oil can be any API Group I, II, III, IV or V base oil.
  • Group I, II and III base oils are hydrocarbon oils.
  • Group IV base oils are polyalphaolefins (synthetic hydrocarbons).
  • Group V base oils include all other synthetic base oils such as polyalkylene glycols and esters.
  • Group V base oils are SYNALOX 100-30B and UCON OSP- 46.
  • conventional polyalkylene glycols (Group V) base oils are used in the present invention.
  • one embodiment includes a butanol initiated propoxylate (SYNALOX 100-30B) and another embodiment includes an oil soluble polyalkylene glycol such as a dodecanol initiated PO/BO copolymer (UCON OSP-46).
  • Examples of the Group V base oils useful in the present invention are further described in Table I. Examples of the invention in a Group IV (PAO) hydrocarbon base fluid are also 5 shown.
  • PAO Group IV
  • the concentration of the base oil, component (b), present in the lubricant composition of the present invention may be at about >50 % by weight in one embodiment, 10 and generally is in the range of from about >50 wt % to about 99.5 wt % in another
  • the base oil, component (b), of the lubricant composition provides several 15 benefit(s) to the lubricant composition including, for example, the base oil provides the lubricant composition with the desired viscosity, viscosity index, and low temperature properties; and the base oil acts as a carrier fluid for the additive package.
  • the lubricant composition of the present invention containing a base oil, a hindered phenolic and a poly ether sulphide may also include other optional components or additives including for example one or more of other base oils, other hindered phenolic antioxidants, other polyether sulphides, viscosity index improvers, corrosion inhibitors, yellow metal passivators, foam control agents, extreme pressure additives, anti-wear additives, friction modifiers, pour point depressants, dyes; and mixtures thereof.
  • the lubricant composition of the present invention can also contain other anti-oxidants such as the aminic types, for example, alkylated diphenylamines (ADPA).
  • the concentration of the optional additives added to the lubricant composition of the present invention may range generally from 0 wt % to about 25 wt % in one embodiment, from about 0.01 wt % to about 15 wt % in another embodiment, and from about 0.1 wt % to about 5 wt % in still another embodiment, based on the total weight of the components in the lubricant composition.
  • the optional additive, component (c), may be added to the lubricant composition to provide the lubricant composition with the following benefit(s):
  • corrosion inhibitors will provide ferrous and non-ferrous corrosion inhibition functionality.
  • Viscosity modifiers can improve the viscosity index of the composition.
  • Solvents can provide improved low temperature properties of the lubricant composition.
  • Demulsifiers can provide improved demulsification of the composition.
  • Antiwear and extreme pressure additives can improve the antiwear and extreme pressure properties of the composition.
  • Lubricity additives can improve the friction control properties of the lubricant composition.
  • the process of preparing the lubricant composition of the present invention includes blending or mixing the above components (a) and (b) together to form the lubricant composition.
  • the process and type of equipment used to prepare the lubricant composition of the present invention includes blending or mixing of the above components in conventional mixing equipment or vessels known in the art.
  • the preparation of the lubricant composition of the present invention is achieved by blending, in known mixing equipment, components (a) and (b) and optionally (c) any other desirable additives.
  • the preparation of the lubricant composition of the present invention, and/or any of the steps thereof, may be a batch or a continuous process.
  • All the above compounds of the lubricant composition are typically mixed and dispersed in a vessel at a temperature enabling the preparation of an effective lubricant composition.
  • the temperature during the mixing of the above components may be generally from about 20 °C to about 100 °C in one embodiment, and from about 25 °C to about 60 °C in another embodiment.
  • the process of preparing a lubricant composition of the present invention includes, for example, the steps of (a) adding a base oil to a vessel; (b) adding the additive package described above to the vessel to form a mixture; (c) stirring the mixture in the vessel and heating the vessel to about 50 °C for about 1 hour (hr) until the resulting composition in the vessel is clear and homogeneous; and (d) cooling the vessel and contents to ambient temperature (about 25 °C).
  • the process of preparing a lubricant composition of the present invention includes, for example, the steps of (a) adding a base oil to a vessel; (b) adding the poly ether sulphide while stirring at from about 20 °C to about 50 °C until the mixture in the vessel is clear and homogeneous; (c) adding the hindered phenolic antioxidant while stirring at a temperature of from about 20 °C to about 50 °C until the resulting composition is clear and homogeneous; and (d) cooling the resultant composition to ambient temperature.
  • the process of preparing the lubricant composition of the present invention includes preparing oil soluble S-PAGs using 1,2-butylene oxide as a building block and reacting with a thiodiglycol to a range of molecular weights.
  • the molecular weight of the S-PAG can be in the range of from about 250 g/mol to about 5,000 g/mol in one embodiment, from about 400 g/mol to about 2,000 g/mol in another embodiment, and from about 500 g/mol to about 1,000 g/mol in still another embodiment.
  • the molecular weight of the S-PAG may be measured by the procedure described in ASTM D4274-16 (standard test method for testing polyurethane raw materials: Determination of Hydroxy 1 Numbers of Polyols).
  • thermo-oxidative stability performance property of the lubricant composition can be extended by 100 % or more over the control sample when the compositions are evaluated versus the modified ASTM D2893 (Method B) test described earlier.
  • the lubricant composition of the present invention is advantageously used in applications where oils are used including for example: automobile oils such as engine oils, transmission fluids, and industrial oils such a compressor fluids, gear oils, hydraulic fluids and greases.
  • ASTM D7042 is used to calculate kinematic viscosity.
  • ASTM D4274-05 is used to measure hydroxyl number.
  • compositions of the present invention are designated as "Examples” or abbreviated as “Ex”; and comparative examples are designated as “Comparative Examples” or abbreviated as “Comp. Ex”.
  • the reactor is further heated to 130 °C.
  • a total of 4,750 g propylene oxide (PO) is added to the reactor over 6 hours (hr) until a target kinematic viscosity (e.g., 46 cSt at 40 °C) is reached.
  • a target kinematic viscosity e.g. 46 cSt at 40 °C
  • the oxide feed is stopped and the reactor is kept at 130 °C for 6 hr to allow the remaining propylene oxide to react away.
  • the resulting polyglycol is treated with magnesium silicate and filtered to remove the catalyst.
  • the resultant product prepared by the process above has a kinematic viscosity at 40 °C of 45.8 cSt, (ASTM D7042) a kinematic viscosity at 100 °C of 6.96 cSt (ASTM D7042), a viscosity index of 109 (ASTM D2270) and a hydroxyl number of 188.0 mg KOH/g (ASTM D4274-05).
  • the resultant product's practical molecular weight by hydroxyl number determination is about 600 g/mol (as measured using ASTM D4274- (2016).
  • the reactor is further heated to 130 °C.
  • a total of 2,514 g 1,2 butylene oxide (BO) is added over 6 hr until a target kinematic viscosity (e.g., 46 cSt at 40 °C) is reached.
  • a target kinematic viscosity e.g. 46 cSt at 40 °C
  • the oxide feed is stopped and the reactor is kept at 130 °C for 6 hr to allow the remaining butylene oxide in the reactor to react away.
  • the resulting polyglycol is treated with magnesium silicate and filtered to remove the catalyst.
  • the resultant product has a kinematic viscosity at 40 °C of 50.7 cSt, a kinematic viscosity at 100 °C of 6.80 cSt, a viscosity index of 84, and a hydroxyl number of 179.0 mg KOH/g.
  • the resultant product's practical molecular weight by hydroxyl number determination is about 630 g/mol (as measured using ASTM D4274-(2016).
  • the ASTM D-2893B test method was modified slightly.
  • the two modifications made to the test method were (1) the test time and (2) the method of measuring the ageing of the lubricant test sample.
  • the test time according to the ASTM D-2893B test method is 13 days.
  • a test time of up to 153 days was used.
  • the ageing of the lubricant test sample is measured by the viscosity change of the fluid (lubricant) before and after the 13 days test time.
  • viscosity changes were not measured; but instead, the total acid number change of the lubricant was measured.
  • the modified ASTM D-2893B test method used is further described in more detail in the following Examples and Comparative Examples:
  • the lubricant compositions used in these examples are described in Table II which describes a base oil content and an anti-oxidant package content; and the results of the test performed in the examples.
  • the apparatus used in these examples is accurately described in the ASTM D2893 (2009) Method B.
  • the test lubricant composition (300 mL) is placed in a borosilicate glass tube and heated to 121 °C in dry air.
  • the method of ASTM D2893 asks for the viscosity change to be recorded after 13 days.
  • a modified ASTM D2893 method was used, that is, tracking the ageing of the lubricant was used in the present examples since poly ethers show ageing changes usually through total acid number (TAN) changes versus viscosity changes. Accordingly, the TAN was measured initially.
  • the TAN was measured after 3 days, 7 days, and 14 days; and thereafter, about every 7 days by removing a 5 mL sample from a glass tube containing the lubricant sample and using the method described in ASTM D664 (2011) to test the 5 mL sample.
  • the lubricant composition is considered to have reached an ageing threshold where the composition was deemed to be no longer useful; and the time (in days) to reach that
  • Table II describes the results of oxidative testing of lubricant compositions wherein the base oil is UCON OSP-46, an oil soluble polyalkylene glycol (PO/BO copolymer), and wherein the anti-oxidant package includes a hindered phenolic anti-oxidant (Irganox LI 35) combined with an anti-oxidant performance booster.
  • the base oil is UCON OSP-46, an oil soluble polyalkylene glycol (PO/BO copolymer)
  • the anti-oxidant package includes a hindered phenolic anti-oxidant (Irganox LI 35) combined with an anti-oxidant performance booster.
  • Two different types of polyether sulphides, S-PAG-PO (Examples 1 and 2) and S-PAG-BO-1 (Examples 3 and 4) are described in Table II as the anti-oxidant performance boosters used.
  • Table II describes examples of the boost in anti-oxidant performance that can be achieved when a hindered phenolic anti-oxidant (Irganox L135) is combined with either S-PAG-PO or S-PAG-BO-1 compared to using a hindered phenolic anti-oxidant alone (Comparative Example A).
  • Table III describes the results of oxidative testing of lubricant compositions wherein the base oil is SYNALOX 100-30B, a conventional polyalkylene glycol (PO homo- polymer), and wherein the anti-oxidant package includes a hindered phenolic anti-oxidant (Irganox LI 35) combined with an anti-oxidant performance booster.
  • the base oil is SYNALOX 100-30B, a conventional polyalkylene glycol (PO homo- polymer)
  • the anti-oxidant package includes a hindered phenolic anti-oxidant (Irganox LI 35) combined with an anti-oxidant performance booster.
  • Two different types of polyether sulphides, S-PAG-PO (Examples 5 and 6) and S-PAG-BO-1 (Examples 7 and 8) are described in Table III as the anti-oxidant performance boosters used.
  • Table III describes examples of the boost in anti-oxidant performance that can be achieved when a hindered phenolic anti-oxidant (Irganox L135) is combined with either S-PAG-PO or S-PAG-BO-1 compared to using a hindered phenolic anti-oxidant alone (Comparative Example B).
  • Table III show that lubricant compositions of the present invention containing a hindered phenolic anti-oxidant when treated with S-PAGs at levels of 1 % and 5 % generally performed better than lubricant compositions without the treatment of S-PAGs.
  • Table IV Examples using a synthetic hydrocarbon base oil (PAO)
  • Table IV describes the results of oxidative testing of lubricant compositions wherein the base oil is a hydrocarbon base oil (polyalphaolefin).
  • the anti-oxidant package includes a hindered phenolic anti-oxidant (Irganox LI 35) combined with an anti-oxidant performance booster.
  • Irganox LI 35 hindered phenolic anti-oxidant
  • Three different types of poly ether sulphides, S-P AG-BO- 1 (Examples 9 and 10), S-PAG-BO-2 (Examples 11 and 12) and S-PAG-BO-3 (Examples 13 and 14) are described in Table IV as the anti-oxidant performance boosters used. Each booster has a different viscosity and molecular weight.
  • Table IV shows examples of the boost in antioxidant performance that can be achieved when a hindered phenolic anti-oxidant (Irganox L135) is combined with either S-PAG-BO-1, S-PAG-BO-2 or S-PAG-BO-3 compared to using a hindered phenolic anti-oxidant alone (Comparative Example C).
  • a hindered phenolic anti-oxidant Irganox L135
  • S-PAG-BO-1 S-PAG-BO-2 or S-PAG-BO-3
  • Table IV shows examples of the boost in antioxidant performance that can be achieved when a hindered phenolic anti-oxidant (Irganox L135) is combined with either S-PAG-BO-1, S-PAG-BO-2 or S-PAG-BO-3 compared to using a hindered phenolic anti-oxidant alone (Comparative Example C).
  • the fluid failed the test after 153 days.
  • S-P AG-BO polymers the compositions exceeded 153 days.

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Organic Chemistry (AREA)
  • Lubricants (AREA)
  • Anti-Oxidant Or Stabilizer Compositions (AREA)

Abstract

Cette invention concerne une composition de type pack antioxydant comprenant une combinaison de : (i) au moins un antioxydant phénolique encombré, et (ii) au moins un polyéther sulfure ; une composition lubrifiante comprenant : (a) la composition de type pack antioxydant et (b) au moins une huile de base ; un procédé de préparation de la composition de type pack antioxydant ; et un procédé de préparation de la composition lubrifiante.
PCT/US2017/038240 2016-06-24 2017-06-20 Composition lubrifiante WO2017223030A1 (fr)

Priority Applications (5)

Application Number Priority Date Filing Date Title
US16/310,310 US10844312B2 (en) 2016-06-24 2017-06-20 Lubricant composition
EP17733720.1A EP3475400B1 (fr) 2016-06-24 2017-06-20 Composition lubrifiante
CN201780039000.4A CN109415650B (zh) 2016-06-24 2017-06-20 润滑剂组合物
JP2018566592A JP2019522706A (ja) 2016-06-24 2017-06-20 潤滑剤組成物
BR112018076938A BR112018076938A2 (pt) 2016-06-24 2017-06-20 composições de embalagem antioxidante e de lubrificante, e, processos para preparar uma composição de embalagem antioxidante e de lubrificante.

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201662354292P 2016-06-24 2016-06-24
US62/354,292 2016-06-24

Publications (1)

Publication Number Publication Date
WO2017223030A1 true WO2017223030A1 (fr) 2017-12-28

Family

ID=59227959

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US2017/038240 WO2017223030A1 (fr) 2016-06-24 2017-06-20 Composition lubrifiante

Country Status (6)

Country Link
US (1) US10844312B2 (fr)
EP (1) EP3475400B1 (fr)
JP (1) JP2019522706A (fr)
CN (1) CN109415650B (fr)
BR (1) BR112018076938A2 (fr)
WO (1) WO2017223030A1 (fr)

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1988009366A2 (fr) * 1987-05-22 1988-12-01 The Lubrizol Corporation Produits anti-oxydants
US4894174A (en) * 1987-06-09 1990-01-16 The Lubrizol Corporation Anti-oxidant compositions
WO2017031162A1 (fr) * 2015-08-20 2017-02-23 Dow Global Technologies Llc Lubrifiant comprenant du polyalkylène glycol contenant du soufre

Family Cites Families (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2518245A (en) * 1946-08-24 1950-08-08 Shell Dev Process for preparing copolymers from alkylene glycols and di(hydroxyalkyl) sulfides
US2562144A (en) * 1946-10-28 1951-07-24 Shell Dev Lubricating composition
US3005853A (en) 1959-06-22 1961-10-24 California Research Corp Preparation of mercaptan and sulfide derivatives thereof
NL263086A (fr) * 1960-04-02 1900-01-01
US3201368A (en) * 1960-10-25 1965-08-17 Ferro Corp Polyolefins stabilized with an (alkylphenol) monosulphide and a nickel alkoxide
US5037569A (en) * 1987-05-22 1991-08-06 The Lubrizol Corporation Anti-oxidant products
US5051198A (en) * 1987-06-09 1991-09-24 The Lubrizol Corporation Anti-oxidant compositions containing mercaptothiadiazole or mercaptobenzothiazole derivatives
US5198132A (en) * 1990-10-11 1993-03-30 The Lubrizol Corporation Antioxidant products
ES2139756T3 (es) 1993-09-13 2000-02-16 Infineum Usa Lp Composiciones lubricantes con poder antioxidante mejorado.
WO1997023587A1 (fr) * 1995-12-22 1997-07-03 Japan Energy Corporation Huile de graissage pour moteurs a combustion interne
US5856280A (en) 1996-07-12 1999-01-05 Exxon Research And Engineering Company Sulfur-containing carboxylic acid derivatives to reduce deposit forming tendencies and improve antioxidancy of aviation turbine oils
JPH1150081A (ja) 1997-08-06 1999-02-23 Nippon Oil Co Ltd 潤滑油組成物
EP1468063B1 (fr) 2001-09-21 2017-12-13 Vanderbilt Chemicals, LLC Compositions d'additifs antioxydantes ameliorees et compositions lubrifiantes contenant lesdites compositions antioxydantes
MY132857A (en) * 2002-12-02 2007-10-31 Ciba Holding Inc Liquid phenolic sulphur-containing antioxidants
US7494960B2 (en) 2004-02-03 2009-02-24 Crompton Corporation Lubricant compositions comprising an antioxidant blend
MY145889A (en) * 2004-07-08 2012-05-15 Shell Int Research Lubricating oil composition
WO2008109502A1 (fr) 2007-03-06 2008-09-12 R.T. Vanderbilt Company, Inc. Nouveaux composés molybdène
EP2358924A2 (fr) 2008-11-17 2011-08-24 Basf Se Utilisation de thioglycoléthoxylate en tant qu'inhibiteur de corrosion
CN102282244B (zh) 2009-02-02 2014-10-15 范德比尔特化学品有限责任公司 无灰润滑剂组合物
WO2011068137A1 (fr) * 2009-12-03 2011-06-09 出光興産株式会社 Composition d'huile lubrifiante
JP6073032B2 (ja) 2011-05-16 2017-02-01 ザ ルブリゾル コーポレイションＴｈｅ Ｌｕｂｒｉｚｏｌ Ｃｏｒｐｏｒａｔｉｏｎ タービンおよび液圧システム用の改善された酸化防止性を有する潤滑組成物
US9556394B2 (en) * 2011-06-14 2017-01-31 Dow Global Technologies Llc Natural and synthetic ester-containing lubricants having enhanced hydrolytic stability

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1988009366A2 (fr) * 1987-05-22 1988-12-01 The Lubrizol Corporation Produits anti-oxydants
US4894174A (en) * 1987-06-09 1990-01-16 The Lubrizol Corporation Anti-oxidant compositions
WO2017031162A1 (fr) * 2015-08-20 2017-02-23 Dow Global Technologies Llc Lubrifiant comprenant du polyalkylène glycol contenant du soufre

Also Published As

Publication number Publication date
EP3475400A1 (fr) 2019-05-01
BR112018076938A2 (pt) 2019-08-06
JP2019522706A (ja) 2019-08-15
US10844312B2 (en) 2020-11-24
US20190345408A1 (en) 2019-11-14
CN109415650A (zh) 2019-03-01
EP3475400B1 (fr) 2021-03-17
CN109415650B (zh) 2021-11-16

Similar Documents

Publication Publication Date Title
RU2452766C2 (ru) Стабилизирующие композиции для смазочных веществ
EP2456845B1 (fr) Polyalkylène glycols utiles comme additifs lubrifiants pour des huiles hydrocarbonées des groupes i-iv
US10844312B2 (en) Lubricant composition
EP3732273B1 (fr) Lubrifiant contenant un polyalkylène glycol modifié soluble dans l'huile
US10752860B2 (en) Lubricant composition
US11566200B2 (en) Polyalkylene glycol lubricant compositions
EP3601502B1 (fr) Compositions lubrifiantes synthétiques présentant une stabilité améliorée à l'oxydation
EP4342964A1 (fr) Additifs à pression extrême présentant une corrosion améliorée par le cuivre
WO2019005767A1 (fr) Composition antioxydante pour polyalkylène glycols
JP2023099737A (ja) 潤滑組成物
WO2019005723A1 (fr) Compositions lubrifiantes à faible teneur en cov

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 17733720

Country of ref document: EP

Kind code of ref document: A1

ENP Entry into the national phase

Ref document number: 2018566592

Country of ref document: JP

Kind code of ref document: A

WWE Wipo information: entry into national phase

Ref document number: 112018076938

Country of ref document: BR

NENP Non-entry into the national phase

Ref country code: DE

REG Reference to national code

Ref country code: BR

Ref legal event code: B01A

Ref document number: 112018076938

Country of ref document: BR

Ref country code: BR

Ref legal event code: B01A

Ref document number: 112018076744

Country of ref document: BR

ENP Entry into the national phase

Ref document number: 2017733720

Country of ref document: EP

Effective date: 20190124

ENP Entry into the national phase

Ref document number: 112018076938

Country of ref document: BR

Kind code of ref document: A2

Effective date: 20181221